Hybrid CMC

2 dni temu

Warszawa, Województwo mazowieckie, Polska TRIUM Clinical Consulting NV Pełny etat 180 000 zł - 240 000 zł Umowa

TRIUM Clinical Consulting NV is seeking a CMC Regulatory Affairs specialist to support development, registration, and lifecycle management of medicinal products across Warsaw and Madrid/Barcelona in a hybrid setup. You will combine CMC expertise with client-facing consulting to drive regulatory submissions and GMP documentation.

The role emphasizes delivering high-quality, compliant documentation, resolving CMC questions from Health Authorities, and collaborating with clients and internal teams